ID
11719
Descripción
The purpose of this study is to compare the safety of two different dose regimens of unfractionated heparin (UFH) during a percutaneous coronary intervention (PCI) procedure in patients with UA (unstable angina)/NSTEMI (non ST segment elevation myocardial infarction) who have been initially treated with fondaparinux. https://clinicaltrials.gov/ct2/show/NCT00790907
Link
https://clinicaltrials.gov/ct2/show/NCT00790907
Palabras clave
Versiones (1)
- 28/7/15 28/7/15 -
Subido en
28 de julio de 2015
DOI
Para solicitar uno, por favor iniciar sesión.
Licencia
Creative Commons BY 4.0
Comentarios del modelo :
Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.
Comentarios de grupo de elementos para :
Comentarios del elemento para :
Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.
Eligibility FUTURA/OASIS 8 Acute Coronary Syndrome NCT00790907
Eligibility Criteria
- StudyEvent: ODM
Descripción
Exclusion Criteria
Descripción
Age < 21 years
Tipo de datos
boolean
Alias
- UMLS CUI-1
- C0001779
Descripción
Any contraindication to UFH
Tipo de datos
boolean
Alias
- UMLS CUI-1
- C2825026
- UMLS CUI-2
- C0522473
Descripción
Any contraindication to fondaparinux
Tipo de datos
boolean
Alias
- UMLS CUI-1
- C1098510
- UMLS CUI-2
- C0522473
Descripción
Contraindication for angiography or PCI at baseline
Tipo de datos
boolean
Alias
- UMLS CUI-1
- C1532338
- UMLS CUI-2
- C0522473
Descripción
Contraindication for angiography at baseline
Tipo de datos
boolean
Alias
- UMLS CUI-1
- C0085532
- UMLS CUI-2
- C0522473
Descripción
refractory or recurrent angina associated with dynamic ST-deviation
Tipo de datos
boolean
Alias
- UMLS CUI-1
- C0002962
Descripción
heart failure
Tipo de datos
boolean
Alias
- UMLS CUI-1
- C0018801
Descripción
life-threatening arrhythmias
Tipo de datos
boolean
Alias
- UMLS CUI-1
- C0085612
Descripción
hemodynamic instability
Tipo de datos
boolean
Alias
- UMLS CUI-1
- C0948268
Descripción
Subjects already receiving treatment with enoxaparin for treatment of the qualifying events
Tipo de datos
boolean
Alias
- UMLS CUI-1
- C0206460
Descripción
Subjects already receiving treatment with LMWH for treatment of the qualifying events
Tipo de datos
boolean
Alias
- UMLS CUI-1
- C3536766
Descripción
Subjects already receiving treatment with bivalirudin for treatment of the qualifying events
Tipo de datos
boolean
Alias
- UMLS CUI-1
- C0168273
Descripción
Subjects already receiving treatment with UFH for treatment of the qualifying events
Tipo de datos
boolean
Alias
- UMLS CUI-1
- C2825026
Descripción
Hemorrhagic stroke within the last 12 months.
Tipo de datos
boolean
Alias
- UMLS CUI-1
- C0559159
Descripción
Indication for anti-coagulation other than acute coronary syndrome (ACS) during the index hospitalization.
Tipo de datos
boolean
Alias
- UMLS CUI-1
- C0003281
Descripción
Pregnancy or women of childbearing potential who are not using an effective method of contraception.
Tipo de datos
boolean
Alias
- UMLS CUI-1
- C0549206
Descripción
Co-morbid condition with life expectancy less than 6 months.
Tipo de datos
boolean
Alias
- UMLS CUI-1
- C0679247
Descripción
Currently receiving an experimental pharmacological agent.
Tipo de datos
boolean
Alias
- UMLS CUI-1
- C0304229
Descripción
Revascularization procedure already performed for the qualifying event.
Tipo de datos
boolean
Alias
- UMLS CUI-1
- C0027056
Descripción
Severe renal insufficiency (i.e., estimated creatinine clearance <20 ml/min)
Tipo de datos
boolean
Alias
- UMLS CUI-1
- C1533077
Similar models
Eligibility Criteria
- StudyEvent: ODM
C0522473 (UMLS CUI-2)
C0522473 (UMLS CUI-2)
C0522473 (UMLS CUI-2)
C0522473 (UMLS CUI-2)